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14. Thyroperoxidase gene mutations in congenital goitrous hypothyroidism with total and partial iodide organification defect. Nascimento AC; Guedes DR; Santos CS; Knobel M; Rubio IG; Medeiros-Neto G Thyroid; 2003 Dec; 13(12):1145-51. PubMed ID: 14751036 [TBL] [Abstract][Full Text] [Related]
15. Increased peroxidase activity in Pendred's syndrome with hypothyroidism. Yamamoto M; Saito S; Sakurada T; Yoshida K; Yoshinaga K Tohoku J Exp Med; 1976 Jun; 119(2):103-13. PubMed ID: 951708 [TBL] [Abstract][Full Text] [Related]
16. [Peroxidase and human thyroid hormone synthesis disorders (author's transl)]. Fragu P Sem Hop; 1981 Jun 8-15; 57(21-24):1130-8. PubMed ID: 6267713 [TBL] [Abstract][Full Text] [Related]
17. Congenital hypothyroidism in two cats due to defective organification: data suggesting loosely anchored thyroperoxidase. Sjollema BE; den Hartog MT; de Vijlder JJ; van Dijk JE; Rijnberk A Acta Endocrinol (Copenh); 1991 Oct; 125(4):435-40. PubMed ID: 1659766 [TBL] [Abstract][Full Text] [Related]
18. Goitrous hypothyroidism due to iodide-trapping defect. Saito K; Yamamoto K; Yoshida S; Manabe S; Suzuki M; Takai T; Saito T; Kuzuya T; Moriyama S J Clin Endocrinol Metab; 1981 Dec; 53(6):1267-72. PubMed ID: 6271803 [TBL] [Abstract][Full Text] [Related]
19. Five novel inactivating mutations in the thyroid peroxidase gene responsible for congenital goiter and iodide organification defect. Rivolta CM; Esperante SA; Gruñeiro-Papendieck L; Chiesa A; Moya CM; Domené S; Varela V; Targovnik HM Hum Mutat; 2003 Sep; 22(3):259. PubMed ID: 12938097 [TBL] [Abstract][Full Text] [Related]